|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure. (Orphanet Rare Disease Ontology, Orphanet_1667)|
|Downloads & Tools|
1 genes/proteins associated with the disease Wolcott-Rallison syndrome from the curated CTD Gene-Disease Associations dataset.
|EIF2AK3||eukaryotic translation initiation factor 2-alpha kinase 3||2.88009|